Laube Guido F, Shah Vanita, Stewart Victoria C, Hargreaves Iain P, Haq Mushfequr R, Heales Simon J R, van't Hoff William G
Nephro-urology Unit, Institute of Child Health, University College London Medical School, London, UK.
Pediatr Nephrol. 2006 Apr;21(4):503-9. doi: 10.1007/s00467-006-0005-x. Epub 2006 Mar 1.
We have determined levels of glutathione (GSH), ATP, mitochondrial complex activity and apoptosis rate in proximal tubular cells (PTCs) exfoliated from urine in cystinotic (n=9) and control (n=9) children. Intracellular GSH was significantly depleted in cystinotic PTCs compared with controls (6.8 nmol GSH/mg protein vs 11.8 nmol GSH/mg protein; P<0.001), but there were no significant differences in mitochondrial complex activities or ATP levels under basal conditions. Cystinotic PTCs showed significantly increased apoptosis rate. After PTCs had been stressed by hypoxia, there was further depletion of GSH in cystinotic and control PTCs (2.4 nmol GSH/mg protein vs 7.2 nmol GSH/mg protein; P<0.001). Hypoxic stress led to increased complex I and complex IV activities in control but not in cystinotic PTCs. ATP levels were significantly reduced in cystinotic PTCs after hypoxic stress (12.2 nmol/mg protein vs 26.9 nmol/mg protein; P<0.001). GSH depletion occurs in this in vitro model of cystinotic PTCs, is exaggerated by hypoxic stress and may contribute to reduced ATP and failure to increase complex I/IV activities. Apoptotic rate is also increased, and these mechanisms may contribute to cellular dysfunction in cultured, human cystinotic PTCs.
我们测定了胱氨酸病患儿(n = 9)和对照儿童(n = 9)尿液中脱落的近端肾小管细胞(PTCs)中的谷胱甘肽(GSH)水平、三磷酸腺苷(ATP)水平、线粒体复合物活性和凋亡率。与对照组相比,胱氨酸病PTCs中的细胞内GSH显著减少(6.8 nmol GSH/ mg蛋白 vs 11.8 nmol GSH/ mg蛋白;P<0.001),但在基础条件下,线粒体复合物活性或ATP水平没有显著差异。胱氨酸病PTCs的凋亡率显著增加。在PTCs受到缺氧应激后,胱氨酸病和对照PTCs中的GSH进一步减少(2.4 nmol GSH/ mg蛋白 vs 7.2 nmol GSH/ mg蛋白;P<0.001)。缺氧应激导致对照组PTCs中复合物I和复合物IV的活性增加,但胱氨酸病PTCs中没有。缺氧应激后,胱氨酸病PTCs中的ATP水平显著降低(12.2 nmol/ mg蛋白 vs 26.9 nmol/ mg蛋白;P<0.001)。在这个胱氨酸病PTCs的体外模型中发生了GSH耗竭,缺氧应激使其加剧,这可能导致ATP减少以及复合物I/IV活性无法增加。凋亡率也增加,这些机制可能导致培养的人胱氨酸病PTCs出现细胞功能障碍。